The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
127590921 12759092 1 I 20160830 20160915 20160919 20160919 EXP GB-JNJFOC-20160915227 JANSSEN 41.00 YR A M Y 0.00000 20160919 CN GB GB

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
127590921 12759092 1 PS PREZISTA DARUNAVIR ETHANOLATE 1 Oral U U 21976 800 MG TABLETS
127590921 12759092 2 SS RALTEGRAVIR POTASSIUM RALTEGRAVIR POTASSIUM 1 Oral U 0 400 MG UNSPECIFIED
127590921 12759092 3 SS LAMIVUDINE. LAMIVUDINE 1 Unknown U 0 UNSPECIFIED
127590921 12759092 4 SS NORVIR RITONAVIR 1 Unknown U 0 UNSPECIFIED

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
127590921 12759092 1 Product used for unknown indication
127590921 12759092 2 Product used for unknown indication
127590921 12759092 3 Product used for unknown indication
127590921 12759092 4 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
127590921 12759092 HO

Reactions reported

Event ID CASEID DRUG REC ACT PT
127590921 12759092 Skin ulcer

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

no results found